跳至主要内容
临床试验/CTRI/2021/10/037428
CTRI/2021/10/037428尚未招募不适用

A comparative study between different doses of intravenous Dexmedetomidine in attenuation of pressor response to laryngoscopy and endotracheal intubation.

Dr Waseema Kabeer1 个研究点 分布在 1 个国家目标入组 80 人开始时间: 2021年1月11日最近更新:

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
80
试验地点
1
主要终点
To observe the attenuation of pressor response to laryngoscopy and endotracheal intubation with IV dexmedetomindine

研究概览

简要总结

It is a randomised,prospective,comparative,double blinded, observational study wherein Two doses of IV dexmeditomidine are compared for the attenuation of hemodynamic pressor response of laryngoscopy and endotracheal intubation before any surgical procedure in the operation theatre.

研究设计

研究类型
Interventional
分配方式
Computer generated randomization
盲法
Participant, Investigator, Outcome Assessor and Date-entry Operator Blinded

入排标准

年龄范围
18.00 Year(s) 至 60.00 Year(s)(—)
性别
All

入选标准

  • Age between 18-60 yr of either sex.
  • ASA grade I and grade II.
  • Patients posted for elective surgeries under general anesthesia requiring intubation.
  • Hemodynamically stable patients having all routine investigations within normal limits.
  • Patients who give written informed consent and are willing to be part of the study.

排除标准

  • Patients refusal.
  • Patients with ASA physical status III and more.
  • Patients with any pre-existing cardiovascular disease.
  • Patients with h/o allergy to test drugs.
  • Patients posted for emergency surgeries.
  • Patients with difficult airway.
  • Patients with neurological disorders and muscle diseases.

结局指标

主要结局

To observe the attenuation of pressor response to laryngoscopy and endotracheal intubation with IV dexmedetomindine

时间窗: PRE SCOPE, AT THE TIME OF SCOPY, 0 MINS, 5 MINS, EVERY 5 MINUTES UPTO 2 HOURS, POST EXTUBATION VAS

次要结局

  • To observe the attenuation of pressor responses to laryngoscopy and endotracheal intubation with intravenous Dexmeditomidine 1mcg/kg(PRE SCOPE, AT THE TIME OF SCOPY, 0 MINS, 5 MINS, EVERY 5 MINUTES UPTO 2 HOURS, POST EXTUBATION VAS)

研究者

发起方
Dr Waseema Kabeer
申办方类型
Other [self]

研究点 (1)

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